In Situ Formation ofN-Trifluoroacetoxy Succinimide (TFA-NHS): One-Pot Formation of Succinimidyl Esters,N-Trifluoroacetyl Amino Acid Succinimidyl Esters, andN-Maleoyl Amino Acid Succinimidyl Esters

2011 ◽  
Vol 76 (21) ◽  
pp. 9169-9174 ◽  
Author(s):  
Nicholas M. Leonard ◽  
Jarmila Brunckova
Keyword(s):  
One Pot ◽  
2016 ◽  
Vol 14 (2) ◽  
pp. 556-563 ◽  
Author(s):  
Veladi Panduranga ◽  
Girish Prabhu ◽  
Roopesh Kumar ◽  
Basavaprabhu Basavaprabhu ◽  
Vommina V. Sureshbabu

A simple and efficient method for the synthesis of N,N’-orthogonally protected imide tethered peptidomimetics is presented. The imide peptidomimetics were synthesized by coupling the in situ generated selenocarboxylate of Nα-protected amino acids with Nα-protected amino acid azides in good yields.


CCS Chemistry ◽  
2020 ◽  
pp. 2764-2771
Author(s):  
Bao-Gui Cai ◽  
Shuai-Shuai Luo ◽  
Lin Li ◽  
Lei Li ◽  
Jun Xuan ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 50 (09) ◽  
pp. 1891-1900 ◽  
Author(s):  
Nina Nedolya ◽  
Boris Trofimov ◽  
Olga Tarasova ◽  
Alexander Albanov

A synthetically simple and convenient approach to tetrasubstituted thiophenes with rare combination of the alkoxy, amino, and cyano groups has been developed. The assembly of polyfunctionalized thiophene ring is implemented in one preparative step by sequential addition of isothiocyanate and 2-bromoacetonitrile to the lithiated (with n-BuLi) alkoxyallene. The reaction proceeds through in situ formation and intramolecular cyclization of cyanomethyl 2-alkoxy-N-buta-2,3-dienimidothioate (1-aza-1,3,4-triene).


2013 ◽  
Vol 214 (10) ◽  
pp. 1114-1121 ◽  
Author(s):  
Natalya Dolya ◽  
Oscar Rojas ◽  
Sabine Kosmella ◽  
Brigitte Tiersch ◽  
Joachim Koetz ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (5) ◽  
pp. 893 ◽  
Author(s):  
Liang Chen ◽  
Huajian Zhu ◽  
Jiang Wang ◽  
Hong Liu

A facile and eco-friendly method has been developed for the synthesis of imidazoles and thiazoles from ethylarenes in water. The reaction proceeds via in situ formation of α-bromoketone using NBS as a bromine source as well as an oxidant, followed by trapping with suitable nucleophiles to provide the corresponding products in good yields under metal-free conditions.


1992 ◽  
Vol 57 (21) ◽  
pp. 5768-5771 ◽  
Author(s):  
Daniel A. Singleton ◽  
Jose P. Martinez ◽  
Grace M. Ndip

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